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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1247410 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
; j% {) u3 T) a$ J3 N8 ]& F: QNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 - O* R3 q# Q7 N3 q5 k% V! c& X9 _
+ Author Affiliations
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9 U2 I8 S* K/ h4 K0 K% S1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 8 x' b4 C$ X1 r+ N
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan # u8 d+ S; K  k* {6 Z: g5 r
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* n0 ~( n8 w$ s0 i0 O+ V2 V$ j2 k$ c4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
+ e# c) e& P# [+ I. H; q! v5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
& @1 L+ W$ I& e# v9 N1 O% Z6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
4 u% _" j% z' i7Kinki University School of Medicine, Osaka 589-8511, Japan
6 A: e' Y4 U# x5 Q8Izumi Municipal Hospital, Osaka 594-0071, Japan
. G4 ]" A9 M/ p, c9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan & \# t, e. x  p( Y6 M
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp 3 \2 p1 p) `: P; w* q! E
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type - x" E, q1 c2 @3 Y# O* N3 r
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
- V% G6 e- g- _( d0 v
, U4 s" J2 p. u1 R6 ~& nAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011
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$ W+ |8 Q" u: N1 G9 YDoi: 10.3892/ol.2011.507
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Pages: 405-410 $ s. `2 T$ j( \, W
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Abstract:4 [7 t# \/ b: B" Q! D  {0 i4 e( Z
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.. W  x& |* A& S! Z

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population1 l/ r6 R; h& R* @8 b' f) S
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* o8 c: |. E3 v! p  i1 c8 C+ Author Affiliations
" H2 ~* q% c; L1 d4 N! S1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
' h( W) V- c7 ^) k. i% l% {* j2Department of Thoracic Surgery, Kyoto University, Kyoto 0 f" Q. v1 F& D" S: c6 r
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
7 l0 X* \% ]: v, p6 B& m&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
4 U; f& M$ K* O  X. dReceived September 3, 2010.
' P& p2 O  l" FRevision received November 11, 2010. 6 g/ I8 y" c5 y. v* P7 m9 v
Accepted November 17, 2010.
. y5 C! S- Z4 ?9 j) J) d( Y6 k, IAbstract: ~2 w) S1 K' f+ h5 U) D( x/ y3 v
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. : D, p; P; G- U/ d0 O
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 0 J& `9 {' I6 r$ w& M- n; d- h
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. # ^0 Y( Z( g% F4 f3 }0 n/ j( ~
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 Y2 R( O7 \& l  c/ }
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。  z9 u* L8 Z7 O& k" v6 o& h/ J3 V/ i
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
0 F' J5 t8 l5 `" D- J4 \* ~http://clinicaltrials.gov/ct2/show/NCT01523587* |0 c' S, ^" _8 I
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
: m" x* V3 e" uhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 * }) o' c$ P( q- `. ?8 E
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。! D/ P" a, S9 x; j. i% z
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
7 x1 Z3 Y# p" @8 L) V8 z从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。, @9 P8 c2 o% ?2 D0 z% ~% K$ b
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。$ x% q5 I! p8 k/ j% s6 a1 B
不错。

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